| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:30379529-30379641 | Rare:30 | ||||
| chr17:30824608-30824875 | Common:3; Rare:109 | ||||
| chr17:30831880-30832010 | Rare:45 | ||||
| chr17:30906205-30906327 | Common:1; Rare:37 | ||||
| chr17:31095072-31095311 | Rare:74; Clinvar:6; Clinvar (benign):1 | ||||
| chr17:31297171-31297343 | Rare:28 | ||||
| chr17:31321577-31321786 | Common:3; Rare:32 | ||||
| chr17:32142367-32142709 | Common:8; Rare:138 | ||||
| chr17:32350038-32350198 | Rare:86 | ||||
| chr17:32444206-32444518 | Common:2; Rare:101 | ||||
| chr17:32927858-32928222 | Common:2; Rare:122 | ||||
| chr17:34156732-34156896 | Rare:25 | ||||
| chr17:34961474-34961561 | Rare:38 | ||||
| chr17:34980466-34980618 | Common:4; Rare:46 | ||||
| chr17:35242910-35243081 | Rare:57 |